FDA Inspection 1059120 - Microlight Corporation of America - September 06, 2018

FDA Inspection 1059120 for Microlight Corporation of America on September 06, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1059120 for Microlight Corporation of America on September 06, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Microlight Corporation of America

Inspection Date

September 6, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdf9c5d6-a1a2-42d9-869a-e7a94e4f37af

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